Troubleshoot your hydrocracking catalyst test

Catalyst testing in parallel reactors is common practice in hydroprocessing; the accurate control and distribution of gas and liquid makes results are more reliable than ever. Tests are more cost-effective and more options or catalyst systems can be tested and/or run replicate reactors to significantly increase precision on the results. The amount of data generated makes troubleshooting of experiments more complex.

Let’s take a look at an hydrocracking screening test of 8 catalysts loaded in duplicates (16 reactors) as typically performed within refinery catalysts testing projects where small differences are expected.

Start with the basics

In such a test, one or more reactors can be affected. The first check should be if the overall mass balance across all reactors (combined liquid product weight and gas make data) is consistent. The standard deviation between the same catalysts at the same conversion level should not be higher than 2%. If it is higher, re-check the liquid product weights before having a detailed look at the online gas chromatogram (GC) (C1-C12). The peaks retention times can shift and cause differences in the gas make.
TIP: check the total amount of methane formed and compare it with the theoretical amount resulting from the DMDS added to spike the feed to check the calibration factors of the GC. In addition, as a rule of thumb, the amount of C2 formed should be lower compared to C3 and C4 – of course depending strongly on the active component used in the catalyst.

And then go step by step

If the overall mass balance of the 16 reactors is correct but you observe a large deviation between reactors, uneven distribution of the liquid or gas is the most likely scenario. This is can be caused by blockages in the upstream feed section. The helium flow mass balance between inlet and outlet across each reactor can be used to validate a working gas feed distribution and should be 100%+-2%.
TIP: check your online GC calibration by comparing the calculations based on the calibrated values with the raw GC chromatogram areas of Helium and Hydrogen (if measured on the same detector) as they should be the same. If the Helium mass balance is correct, verify that the total counts of the FID in the GC between similar reactors is similar; else there is probably an issue with your catalyst. If you have a Flowrence® Active Liquid Distribution (ALD), you can easily identify issues with the liquid distribution; simply monitor the flow signal for each reactor in the ALD flow sensor to validate equal distribution real-time.

More information about our technology can be found here.

3 key graphs you shouldn’t miss on your testing dashboard

  1. Mass Balance vs Time-on-stream – The standard deviation per reactor should be within 2% (95% interval) independent of the conversion. If deviations occur, especially with higher net conversion (resulting in higher gas make) look at the online GC gas quantification.
  2. Hydrogen Consumption vs Net Conversion – The consumption should clearly correlate with the net conversion and increase with increasing temperature. Please note if the hydrogen consumption increases with temperature but the net conversion is stable you probably reached equilibrium and/or the maximum activity of the catalyst is reached.
  3. Individual Hydrocarbon Selectivities vs Net Conversion – These graphs are complex and strongly depend on the catalyst active component. For example, if there is a high gas make with lower than expected conversion, then the unselective cracking towards lighter components is dominating which probably points towards an issue with the zeolitic component.

Conclusion

Being able to troubleshoot a hydrocracking experiment real-time is key to deliver meaningful test results; some considerations are shared above. With the Flowrence® enabled-technology like the ALD (Active Liquid Distribution) and iRPC (individual Reactor Pressure Control), you are able to execute hydrocracking experiments on-time in cost-effectively; accelerating your catalyst R&D.

Flowrence® products specifications

Reactor Section

Easy and quick reactor exchange system. Possibility to use quartz reactors at high pressure.

1 block of 4 reactors

HT = High Temperature max. 800°C nominal, limited to 925°C (<0.5°C reactor to reactor deviation)

4 blocks of 4 reactors

HT  or MT = Medium Temperature max. 525°C (<0.5°C block-to-block deviation)

16 reactors with iRTC

individual Reactor Temperature Control
max. 550°C (<0.5°C reactor-to-reactor)

4 reactors with iRTC

individual Reactor Temperature Control
max. 550°C (<0.5°C reactor-to-reactor)

Temperature Ranges (°C)

100 – 800°C
up 925°C (Option)

50 – 525°C
100 – 800°C
up 925°C (Option)

50 – 550°C

50 – 550°C

Reactor Types

L= Length
OD= Outer Diameter
ID= Inner Diameter
SS= Stainless Steel (< 550⁰C)
Qz= Quartz (< 925⁰C)

L 300 mm 561 mm
OD 3 mm 6 mm
ID SS 2 / 2.6 mm 2 / 3 / 4 / 5 mm
ID Qz 2 mm 2 / 4 mm
300 mm 561 mm 561 mm
3 mm 3 mm 6 mm
2 / 2.6 mm 2 / 2.6 mm 2 / 3 / 4 / 5 mm
2 mm 2 mm 2 / 4 mm
561 mm
3 mm
2 / 2.6 mm
2 mm
561 mm
3 mm
2 / 2.6 mm
2 mm

Maximum Catalyst Bed Length

(isothermal zone tolerance ± 1°C)
Note: isothermal length is dependent on the temperature range

300 / 3 HT 561 / 6 HT
>120 mm @ 450°C >200 mm @ 500°C
>90 mm @ 800°C >150 mm @ 800°C
>140 mm @ 925°C
300 / 3 HT 561 / 3 MT 561 / 6 HT
>120 mm @ 450°C >310 mm @ 450°C >200 mm @ 500°C
>90 mm @ 800°C >150 mm @ 800°C
>140 mm @ 925°C
561 / 3 MT iRTC
250°C ±0.5°C 41cm (4reactors)
350°C±0.5°C 38cm (4reactors)
550°C±0.5°C 28cm (4reactors)
3 reactors at 550°C, 1 reactor 350°C:
550°C=27cm 350°C=41cm ±0.5°C
561 / 3 MT iRTC
250°C ±0.5°C 41cm (4reactors)
350°C±0.5°C 38cm (4reactors)
550°C±0.5°C 28cm (4reactors)
3 reactors at 550°C, 1 reactor 350°C:
550°C=27cm 350°C=41cm ±0.5°C

Catalyst Volume (mL)

(isothermal zone)

0.2 - 0.6 mL 0.4 - 2.0 mL
0.2 - 0.6 mL 0.4 - 1.0 mL 0.4 - 2.0 mL
0.4 - 1.0 mL
0.4 - 1.0 mL

Pressure Ranges (barg)

2 – 80 barg
0.5 – 180 barg (option)

2 – 100 barg
0.5 – 180 barg

2 – 80 barg
0.5 – 180 barg

2 – 20 barg
2 – 50 barg (option)

Reactor Pressure Control

Advanced control RSD ±0.1 barg at reference conditions (gas phase only and 20 barg). For trickle flow Advanced control RSD ±0.5barg.

Standard (±0.5 barg)
Advanced (±0.1 barg) (option)

Standard (±0.5 barg)
Advanced (±0.1 barg) (option)

Advanced (±0.1 barg)

Advanced (±0.1 barg)

Gas Feed Lines

(#Gas Feeds)

Up to 6 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 7 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 7 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Up to 6 + Diluent gas

He, Ar, N2, H2, CH4, CO2, C2H4, C2H6, O2/Inert (≤5%), CO, Other gases

Online Analysis

Full integration GC, MS , GC/MS with data visualisation (option)

Full integration GC, MS , GC/MS with data visualisation

Full integration GC, MS , GC/MS with data visualisation

Full integration GC, MS , GC/MS with data visualisation

Liquid Feed

 Split feeding 8 + 8 reators (option)

Pump-Coriolis dosing system
(ambient, cooled)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Pump-Coriolis dosing system
(ambient, cooled, heated 80°C)

Liquid Distribution

Microfluidic Distribution
(4-channel glass-chip)

Microfluidics Distribution
(4x4-channel glass-chip)
(16-channel glass-chip)
Active Liquid Distribution (option)
(with automatic isolation valves)

Active Liquid Distribution
(with automatic isolation valves)

Microfluidic Distribution
(4-channel glass-chip)

Liquid Sampling

(G/L Separation)

Parallel liquid sampling (4 x 20ml vials) with sequential on-line gas phase sampling (option)

Automated liquid sampling (4 rows x 16 vials x 8ml) with sequential on-line gas phase sampling (option)

Automated liquid sampling (4 rows x 16 vials x 8ml) with sequential on-line gas phase sampling (option)

Parallel liquid sampling (4 x 20ml vials) with sequential on-line gas phase sampling (option)

Reactors Effluent Handling

(Off-line Analysis Connection)

Full heated circuit up to 180°C with sequential on-line full gas phase sampling (option)

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Full heated circuit up to 200°C with sequential on-line full gas phase sampling

Offline Analysis

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode (option)

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Integrated Workflow: SimDist, total S/N, liquid density, balance, label printer, barcode

Waste Handling

Ambient temperature
Heated wax trapping (option)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Ambient temperature / Cooled containers / Heated compartment (wax trapping, heavies)

Safety

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Gas sensors and control box (CO, LEL, VOC)

Flowrence® Software

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Flowrence® recipe builder, control & database builder

Microfluidics modular gas distribution

Unrivalled accuracy in gas distribution with patented glass-chips for 4 and 16 reactors, with a guaranteed flow distribution of 0.5% RSD. Quick exchange of glass-chips for different operating conditions. Flexibility to cover a wide range of applications.

TinyPressure glass-chip holder with integrated pressure measurement

Compact modular design for gas and liquid distribution. No high-temperature pressure sensors required. Quick exchange of the microfluidic glass-chips, without the need for time-consuming leak testing.

Tube-in-tube reactor technology with effluent dilution

Unique tube-in-tube design with easy and rapid exchange of the reactor tubes (within minutes!). No need for any connections. Use of inert diluent gas (outside of reactor) to maintain the pressure prevents dead volumes and back flow. Possibility to use quartz reactors at high pressure applications.

Automated liquid sampling system

Programmable, fully automated liquid product sampling robot for 24/7 hands-off operation. Robot equipped with a compact manifold aiming at depressurizing the effluent immediately after each reactor to atmospheric pressure. Eliminates the use of high pressure valves.

Reactor Pressure Control (RPC)

The most accurate and stable pressure regulator for a 16-parallel reactors with just ±0.1bar RSD. The RPC uses microfluidics technology to regulate the pressure of each reactor, maintaining equal distribution of the inlet flow over the 16 reactors.

Auto-calibrating liquid feed distribution, measurement, and control

Distribution of difficult feedstocks e.g., VGO, HVGO, DAO. Liquid distribution 0.2% RSD, making it the most accurate liquid distribution device on the market. Option to selectively isolate each reactor.

Single-Pellet-String-Reactors (SPSR)

No dead-zones, no bed packing & distribution effects. The catalyst packing is straightforward and does not require special procedures. A single string of catalyst particles is loaded in the reactors avoiding maldistribution, eliminating channeling and incomplete wetting.

EasyLoad®

Unique reactor closing system with no connections. Rapid reactor replacement minimizing delays, improving uptime and reliability. Stable evaporation by liquid injection into reactor.

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